Non-Small Cell Lung Cancer (NSCLC) Pipeline Analysis Report

Non-Small Cell Lung Cancer (NSCLC) Pipeline Analysis Report


Non-Small Cell Lung Cancer (NSCLS) Drug Pipeline Analysis 2024 The drug pipeline is significantly driven by the increasing prevalence of non-small cell lung cancer (NSCLC), which accounts for approximately 85% of all lung cancer cases. Globally, lung cancer affects over 2.2 million people annually, making it one of the leading causes of cancer-related deaths. In the United States alone, around 238,340 new cases of lung cancer are expected to be diagnosed in 2024, with NSCLC comprising most of these cases. This high incidence highlights the urgent need for effective treatment options and drives ongoing research and development efforts in NSCLC therapies. Key Takeaways • The non-small cell lung cancer (NSCLC) drug pipeline market includes key players such as AstraZeneca PLC, Novartis AG, Cipla BioTec Pvt. Ltd., Bristol-Myers Squibb Company, GSK Plc, Pfizer, Inc., and NovoCure GmbH. These companies are at the forefront of developing groundbreaking therapies to address NSCLC effectively. • The NSCLC drug pipeline includes promising candidates such as osimertinib, pembrolizumab, nivolumab, and atezolizumab, among others. These therapies are at various stages of development and offer new hopes for innovative cancer treatment options. • Regulatory agencies are providing support through expedited pathways for drug approvals and designations, encouraging rapid development and market availability of new therapies. Report Coverage The NSCLC drug pipeline analysis provides an overview of recent advancements and ongoing clinical trials. The report highlights progress in targeted therapies and immunotherapies, aiming for improved survival rates and quality of life. It covers innovative approaches such as checkpoint inhibitors that enhance immune response and antibody-drug conjugates that deliver cytotoxic agents directly to cancer cells. The competitive landscape examines collaborations and strategic partnerships that accelerate R&D. It also discusses regulatory milestones achieved by investigational drugs, highlighting their impact on future treatment paradigms, and promising more effective and personalized treatment options for NSCLC patients. Non-Small Cell Lung Cancer (NSCLS) Drug Pipeline Outlook NSCLC is one of the most prevalent types of lung cancer, characterized by abnormal growth of cells in lung tissue. It accounts for approximately 85% of all lung cancer cases and can be categorized into subtypes such as adenocarcinoma, squamous cell carcinoma, and large cell carcinoma. The disease often progresses silently until it reaches advanced stages, making early detection and treatment challenging. Treatment strategies often involve a combination of surgery, chemotherapy, radiation, targeted therapy, and immunotherapy. Advancements in targeted therapies and immune checkpoint inhibitors are enhancing NSCLC treatment, offering promising long-term outcomes. The market is witnessing increased investment in R&D and regulatory approvals for innovative drugs, underscoring a dynamic landscape focused on improving survival rates and patient care. In 2024, significant advancements in breast cancer treatment have been made. The FDA recently approved Alectinib (Alecensa), as an adjuvant treatment for patients with ALK-positive NSCLC following tumor resection. This approval was based on the ALINA trial, which demonstrated significant improvements in disease-free survival compared to chemotherapy. These approvals and ongoing developments underscore the dynamic and evolving nature of non-small cell lung cancer (NSCLS), offering new treatment options and hope for improved patient outcomes. Non- Small Cell Lung Cancer (NSCLS)- Pipeline Drug Profiles Recent developments in NSCLC treatment have introduced several promising drugs currently in clinical trials: • Sasanlimab: A PD-1 inhibitor under investigation for its potential to enhance anti-tumor immune responses in NSCLC, aiming to improve progression-free and overall survival rates. • HER3-DXd: An antibody-drug conjugate targeting HER3, designed to deliver cytotoxic agents directly to cancer cells, showing promise in HER3-expressing tumors. • Osimertinib: A third-generation EGFR inhibitor used for the treatment of EGFR-mutated NSCLC, showing efficacy in both early and advanced stages of the disease. • Pembrolizumab (MK-3475): A PD-1 inhibitor used in various settings for NSCLC, known for its role in improving survival outcomes when used as a monotherapy or in combination with chemotherapy. Drug Pipeline Therapeutic Assessment This section of the report covers the analysis of non-small cell lung cancer (NSCLS) drugs based on various segmentations such as: Analysis by Route of Administration • Oral The oral route of administration in NSCLC treatment involves medications such as osimertinib (Tagrisso) and lorlatinib (Lorbrena), which are designed to target specific genetic mutations like EGFR and ALK, respectively. These oral therapies provide convenient at-home treatment options, allowing patients to maintain their daily routines without frequent hospital visits. This approach improves patient compliance and adherence to treatment regimens, making it particularly beneficial for targeted therapies that require consistent dosing over long periods. The non-invasive nature of oral medications offers a significant advantage for managing NSCLC effectively. • Parenteral Intravenous (IV) administration is a common route for delivering NSCLC treatments, including immunotherapies like pembrolizumab (Keytruda) and nivolumab (Opdivo). These monoclonal antibodies are administered directly into the bloodstream, ensuring rapid and efficient delivery of the therapeutic agents to the tumor sites. IV administration is crucial for immunotherapy regimens in advanced stages of NSCLC, where precise and potent delivery is necessary to achieve optimal therapeutic outcomes. This method allows for controlled dosage and immediate action, which is essential for managing aggressive cancer forms. • Others Other delivery methods being explored for NSCLC include inhalation therapies and localized delivery techniques. Inhalation therapies aim to administer drugs directly to the lungs, enhancing the concentration of therapeutic agents at tumor sites while minimizing systemic exposure. This approach can potentially improve efficacy by delivering higher doses directly to the cancer cells, reducing side effects commonly associated with systemic drug distribution. Novel localized delivery methods, such as intratumoral injections, are also being investigated to provide targeted treatment that maximizes the therapeutic impact on the tumor. Analysis by Phase According to EMR analysis, Phase II clinical trials dominate the non-small cell lung cancer (NSCLS) pipeline. The number of non-small cell lung cancer (NSCLS) drugs currently in Phase 2 clinical trials varies as new trials are continually initiated and completed. However, as of the latest data, there are over 3000 ongoing Phase 2 trials for non-small cell lung cancer (NSCLS) drugs worldwide. These trials involve a wide range of therapeutic approaches, including targeted therapies, immunotherapies, and combination treatments. • Preclinical Phase: Laboratory and animal studies to assess safety and efficacy. • Phase I: Small-scale human trials focusing on safety and dosage. • Phase II: Larger trials to evaluate efficacy and side effects. • Phase III: Large-scale trials to confirm effectiveness, monitor side effects, and compare with standard treatments. • Phase IV: Post-marketing studies to gather more information on risks, benefits, and optimal use. Analysis by Drug Class • Small Molecule Small molecule drugs, such as crizotinib (Xalkori) and lorlatinib (Lorbrena), are designed to target specific genetic mutations in NSCLC, like ALK and ROS1 rearrangements. These drugs penetrate cell membranes easily due to their low molecular weight, enabling them to interfere directly with intracellular signaling pathways that drive cancer growth. This targeted approach provides personalized treatment options, allowing for more effective management of NSCLC in patients with specific genetic profiles. These therapies have significantly improved outcomes by offering tailored treatments that address the underlying genetic causes of the disease (FDA) (Cancer Network). • Polymer Polymeric drug delivery systems are used to enhance the stability and bioavailability of chemotherapeutic agents like docetaxel. These systems encapsulate drugs within biodegradable polymers, protecting them from degradation and allowing for controlled release at the tumor site. This method improves the therapeutic index by enabling higher drug concentrations to reach the tumor while minimizing systemic toxicity. By enhancing drug solubility and reducing side effects, polymer-based delivery systems represent an important advancement in cancer treatment. • Monoclonal Antibody Monoclonal antibodies, such as atezolizumab (Tecentriq) and durvalumab (Imfinzi), work by blocking interactions between PD-L1 on cancer cells and PD-1 on immune cells. This blockade enhances the body's immune response against cancer by preventing tumor cells from evading immune detection. These agents are crucial in immunotherapy regimens for NSCLC, helping to stimulate immune-mediated tumor cell destruction and improve survival rates in patients with advanced disease. • Peptides Peptide-based agents are being developed to disrupt cancer cell signaling pathways, offering novel mechanisms to inhibit tumor growth. These peptides can interfere with protein-protein interactions essential for cancer cell survival, leading to apoptosis and reduced tumor proliferation. By targeting specific signaling cascades, peptide therapies provide an additional strategy for managing NSCLC, with the potential for lower toxicity compared to traditional chemotherapeutics. • Gene Therapy Gene therapy involves using viral or non-viral vectors to deliver genetic material that can correct mutations or enhance immune responses in NSCLC. These innovative approaches aim to directly modify the genetic drivers of cancer or to introduce genes that boost the immune system's ability to fight cancer. Although still largely experimental in NSCLC, gene therapy holds promise for providing personalized and potentially curative treatments by addressing the root genetic causes of cancer. Non-Small Cell Lung Cancer (NSCLS) Drug Clinical Trials Assessment- Competitive Dynamics Here are a few notable participants involved in non-small cell lung cancer (NSCLS) research and development: These advancements represent significant steps forward in non-small cell lung cancer (NSCLS) treatment, potentially offering patients more effective and less burdensome options. AstraZeneca PLC AstraZeneca, headquartered in Cambridge, UK, is a global leader in oncology research and development, focusing on targeted therapies and immunotherapies for NSCLC. The company's portfolio includes osimertinib (Tagrisso), an EGFR inhibitor that targets specific genetic mutations in NSCLC, and durvalumab (Imfinzi), a PD-L1 inhibitor that enhances immune responses. AstraZeneca's pipeline emphasizes precision medicine and innovative treatment approaches, aiming to improve patient outcomes through cutting-edge research. Novartis AG Novartis, based in Basel, Switzerland, is a prominent player in cancer treatment innovation, developing therapies for NSCLC that target genetic mutations and immune pathways. The company's key offerings include capmatinib (Tabrecta), a MET inhibitor for NSCLC with MET exon 14 skipping mutations, and ceritinib (Zykadia), which targets ALK-positive tumors. Novartis is committed to advancing personalized medicine, focusing on therapies that address the unique molecular profiles of NSCLC patients. Cipla BioTec Pvt. Ltd. Cipla BioTec, headquartered in Mumbai, India, is actively engaged in the development of biosimilars and novel therapeutics for NSCLC. The company leverages its expertise in biotechnology to produce cost-effective, high-quality cancer treatments, including biosimilar versions of monoclonal antibodies. Cipla BioTec's research focuses on improving access to advanced cancer therapies, aiming to make innovative treatments more widely available to patients globally. Bristol-Myers Squibb Company Bristol-Myers Squibb, headquartered in New York City, is at the forefront of immunotherapy development for NSCLC. The company has developed nivolumab (Opdivo), a PD-1 inhibitor that enhances immune system activity against cancer cells. Bristol-Myers Squibb's research is dedicated to overcoming treatment resistance and improving survival outcomes for patients with advanced NSCLC, utilizing its robust pipeline of immuno-oncology agents. Other key players in the market include GSK Plc., Pfizer, Inc., and NovoCure GmbH. Reasons To Purchase This Report The non-small cell lung cancer (NSCLS) drug pipeline analysis report offers invaluable insights into the latest advancements and future trends in non-small cell lung cancer (NSCLS) treatment. It provides detailed evaluations of emerging therapies, pipeline assessment, and competitive landscape analysis, enabling informed investment decisions and strategic planning. Key Questions Answered in the Non-Small Cell Lung Cancer (NSCLS) Drug Pipeline Analysis Report • What is the current state of the non-small cell lung cancer (NSCLS) drug pipeline? • How many companies are currently involved in non-small cell lung cancer (NSCLS) drug development? • What is the number of drugs in Phase III and Phase IV trials for non-small cell lung cancer (NSCLS)? • Which organisations are at the forefront of non-small cell lung cancer (NSCLS) drug research? • What are the effectiveness and safety profiles of the drugs in the non-small cell lung cancer (NSCLS) pipeline? • What opportunities and challenges exist in the non-small cell lung cancer (NSCLS) clinical trial landscape? • Which companies are leading the major clinical trials for non-small cell lung cancer (NSCLS) drugs? • Which regions are involved in clinical trials for non-small cell lung cancer (NSCLS)? • What are the recent clinical trial results for non-small cell lung cancer (NSCLS) drugs? • What are the emerging trends in non-small cell lung cancer (NSCLS) clinical trials?


1 Preface
1.1 Introduction
1.2 Objectives of the Study
1.3 Research Methodology and Assumptions
2 Executive Summary
3 Overview of Non-Small Cell Lung Cancer (NSCLC)
3.1 Signs and Symptoms
3.2 Causes
3.3 Risk Factors
3.4 Types of Non-Small Cell Lung Cancer (NSCLC)
3.5 Diagnosis
3.6 Treatment
4 Patient Profile
4.1 Patient Profile Overview
4.2 Patient Psychology and Emotional Impact Factors
4.3 Risk Assessment and Treatment Success Rate
5 Non-Small Cell Lung Cancer (NSCLC): Epidemiology Snapshot
5.1 Non-Small Cell Lung Cancer (NSCLC) Incidence by Key Markets
5.2 Non-Small Cell Lung Cancer (NSCLC)– Patients Seeking Treatment in Key Markets
6 Non-Small Cell Lung Cancer (NSCLC): Market Dynamics
6.1 Market Drivers and Constraints
6.2 SWOT Analysis
7 Non-Small Cell Lung Cancer (NSCLC): Key Facts Covered
7.1 Top Countries Contributing to Clinical Trials in Asia-Pacific
7.2 Top Countries Contributing to Clinical Trials in Europe
7.3 Top Countries Contributing to Clinical Trials in North America
7.4 Top Countries Contributing to Clinical Trials in Other Regions
8 Non-Small Cell Lung Cancer (NSCLC), Drug Pipeline Assessment
8.1 Assessment by Treatment Type
8.2 Assessment by Route of Administration
8.3 Assessment by Drug Class
9 EMR Drug Pipeline Comparative Analysis
9.1 List of Non-Small Cell Lung Cancer (NSCLC) Pipeline Drugs
9.1.1 By Company
9.1.2 By Phase
9.1.3 By Indication
9.1.4 By Trial Status
9.1.5 By Funder Type
9.2 EMR Attribute Scoring Analysis of Pipeline Drugs (Top Drugs)
10 Non-Small Cell Lung Cancer (NSCLC) Drug Pipeline - Late-Stage Products (Phase III and IV) (Top Drugs)
10.1 Comparative Analysis for Late-Stage Drugs
10.1.1 Study Type
10.1.2 Recruitment Status
10.1.3 Company
10.1.4 Funder Type
10.2 Product Level Analysis*
10.2.1 Durvalumab
10.2.1.1 Product Description
10.2.1.2 Trial ID
10.2.1.3 Sponsor Name
10.2.1.4 Study Type
10.2.1.5 Drug Class
10.2.1.6 Eligibility Criteria
10.2.1.7 Study Record Dates
10.2.1.7.1 First Submitted
10.2.1.7.2 First Posted
10.2.1.7.3 Last Update Posted
10.2.1.7.4 Last Verified
10.2.1.8 Indication
10.2.1.9 Study Design
10.2.1.10 Recruitment Status
10.2.1.11 Enrollment (Estimated)
10.2.1.12 Location Countries
10.2.1.13 Recent Results
10.2.2 Capmatinib
10.2.3 MEDI4736
10.2.4 TG4010
10.2.5 Other Drug
11 Non-Small Cell Lung Cancer (NSCLC) Drug Pipeline - Mid-Stage Products (Phase II) (Top Drugs)
11.1 Comparative Analysis for Mid-Stage Drugs
11.1.1 Study Type
11.1.2 Recruitment Status
11.1.3 Company
11.1.4 Funder Type
11.2 Product Level Analysis*
11.2.1 AZD2936
11.2.1.1 Product Description
11.2.1.2 Trial ID
11.2.1.3 Sponsor Name
11.2.1.4 Study Type
11.2.1.5 Drug Class
11.2.1.6 Eligibility Criteria
11.2.1.7 Study Record Dates
11.2.1.7.1 First Submitted
11.2.1.7.2 First Posted
11.2.1.7.3 Last Update Posted
11.2.1.7.4 Last Verified
11.2.1.8 Indication
11.2.1.9 Study Design
11.2.1.10 Recruitment Status
11.2.1.11 Enrollment (Estimated)
11.2.1.12 Location Countries
11.2.1.13 Recent Results
11.2.2 BPI-361175
11.2.3 ILX651
11.2.4 RAD001
11.2.5 Other Drugs
12 Non-Small Cell Lung Cancer (NSCLC) Drug Pipeline - Early-Stage Products (Phase I) (Top Drugs)
12.1 Comparative Analysis for Early-Stage Drugs
12.1.1 Study Type
12.1.2 Recruitment Status
12.1.3 Company
12.1.4 Funder Type
12.2 Product Level Analysis*
12.2.1 BGB324
12.2.1.1 Product Description
12.2.1.2 Trial ID
12.2.1.3 Sponsor Name
12.2.1.4 Study Type
12.2.1.5 Drug Class
12.2.1.6 Eligibility Criteria
12.2.1.7 Study Record Dates
12.2.1.7.1 First Submitted
12.2.1.7.2 First Posted
12.2.1.7.3 Last Update Posted
12.2.1.7.4 Last Verified
12.2.1.8 Indication
12.2.1.9 Study Design
12.2.1.10 Recruitment Status
12.2.1.11 Enrollment (Estimated)
12.2.1.12 Location Countries
12.2.2 S095018
12.2.3 Anti-Trop2 CAR-NK cell
12.2.4 Other Drugs
13 Non-Small Cell Lung Cancer (NSCLC) Drug Pipeline - Preclinical and Discovery Stage Products (Top Drugs)
13.1 Comparative Analysis for Preclinical and Discovery Stage Drugs
13.1.1 Study Type
13.1.2 Recruitment Status
13.1.3 Company
13.1.4 Funder Type
13.2 Product Level Analysis*
13.2.1 Avelumab
13.2.1.1 Product Description
13.2.1.2 Trial ID
13.2.1.3 Sponsor Name
13.2.1.4 Study Type
13.2.1.5 Drug Class
13.2.1.6 Eligibility Criteria
13.2.1.7 Study Record Dates
13.2.1.7.1 First Submitted
13.2.1.7.2 First Posted
13.2.1.7.3 Last Update Posted
13.2.1.7.4 Last Verified
13.2.1.8 Indication
13.2.1.9 Study Design
13.2.1.10 Recruitment Status
13.2.1.11 Enrollment (Estimated)
13.2.1.12 Location Countries
13.2.2 Pembrolizumab
13.2.3 99mTc-NM-01
13.2.4 MPDL3280A
13.2.5 Other Drugs
14 Non-Small Cell Lung Cancer (NSCLC), Key Drug Pipeline Companies
14.1 AstraZeneca PLC
14.1.1 Company Snapshot
14.1.2 Pipeline Product Portfolio
14.1.3 Financial Analysis
14.1.4 Recent News and Developments
14.2 Novartis AG
14.2.1 Company Snapshot
14.2.2 Pipeline Product Portfolio
14.2.3 Financial Analysis
14.2.4 Recent News and Developments
14.3 Cipla BioTec Pvt. Ltd.
14.3.1 Company Snapshot
14.3.2 Pipeline Product Portfolio
14.3.3 Financial Analysis
14.3.4 Recent News and Developments
14.4 Bristol-Myers Squibb Company
14.4.1 Company Snapshot
14.4.2 Pipeline Product Portfolio
14.4.3 Financial Analysis
14.4.4 Recent News and Developments
14.5 GSK Plc.
14.5.1 Company Snapshot
14.5.2 Pipeline Product Portfolio
14.5.3 Financial Analysis
14.5.4 Recent News and Developments
14.6 Pfizer & Co., Inc.
14.6.1 Company Snapshot
14.6.2 Pipeline Product Portfolio
14.6.3 Financial Analysis
14.6.4 Recent News and Developments
14.7 NovoCure GmbH
14.7.1 Company Snapshot
14.7.2 Pipeline Product Portfolio
14.7.3 Financial Analysis
14.7.4 Recent News and Developments
15 Regulatory Framework for Drug Approval, By Region
16 Terminated or Suspended Pipeline Products
*Complete list of drugs covered will be provided in the report.
The EMR team aims to provide comprehensive coverage of the Top Drugs for each Phase, considering factors such as the company's financial standing, geographic presence, and market position to ensure thorough analysis in this section.

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